Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA09g29220 | A09 | 19362903 | G | A | upstream_gene_variant | MODIFIER | c.-2478G>A| |
S162 |
2 | BAA09g29220 | A09 | 19362968 | C | T | upstream_gene_variant | MODIFIER | c.-2413C>T| |
S183 S198 |
3 | BAA09g29220 | A09 | 19363194 | G | A | upstream_gene_variant | MODIFIER | c.-2187G>A| |
S132 S137 S215 |
4 | BAA09g29220 | A09 | 19363883 | C | T | upstream_gene_variant | MODIFIER | c.-1498C>T| |
S25 S264 |
5 | BAA09g29220 | A09 | 19364001 | G | A | upstream_gene_variant | MODIFIER | c.-1380G>A| |
S202 |
6 | BAA09g29220 | A09 | 19364259 | C | T | upstream_gene_variant | MODIFIER | c.-1122C>T| |
S243 S299 |
7 | BAA09g29220 | A09 | 19365734 | G | A | missense_variant | MODERATE | c.284G>A|p.Arg95His |
S157 S163 |
8 | BAA09g29220 | A09 | 19365763 | G | A | missense_variant | MODERATE | c.313G>A|p.Val105Ile |
S192 |
9 | BAA09g29220 | A09 | 19365845 | C | T | intron_variant | MODIFIER | c.328-10C>T| |
S8 |
10 | BAA09g29220 | A09 | 19366139 | G | A | missense_variant | MODERATE | c.511G>A|p.Asp171Asn |
S15 S3 |
11 | BAA09g29220 | A09 | 19366248 | G | A | missense_variant | MODERATE | c.620G>A|p.Arg207Lys |
S138 |
12 | BAA09g29220 | A09 | 19366681 | G | A | downstream_gene_variant | MODIFIER | c.*201G>A| |
S259 |
13 | BAA09g29220 | A09 | 19366876 | C | T | downstream_gene_variant | MODIFIER | c.*396C>T| |
S283 |
14 | BAA09g29220 | A09 | 19367269 | G | A | downstream_gene_variant | MODIFIER | c.*789G>A| |
S138 |
15 | BAA09g29220 | A09 | 19368008 | C | T | downstream_gene_variant | MODIFIER | c.*1528C>T| |
S40 |
16 | BAA09g29220 | A09 | 19368213 | C | T | downstream_gene_variant | MODIFIER | c.*1733C>T| |
S278 |
17 | BAA09g29220 | A09 | 19370261 | C | T | downstream_gene_variant | MODIFIER | c.*3781C>T| |
S183 S198 |